Proximogram—A multi-omics network-based framework to capture tissue heterogeneity integrating single-cell omics and spatial profiling

The increasing availability of patient-derived multimodal biological data for various diseases has opened up avenues for finding the optimal methods for jointly leveraging the information extracted in a customizable and scalable manner. Here, we propose the Proximogram, a graph-based representation that provides a joint construct for embedding independently obtained omics and spatial data. To evaluate the representation, we generated proximograms from 2 distinct biological sources, namely, multiplexed immunofluorescence images and single-cell RNA-seq data obtained from patients across two pancreatic diseases that include normal and chronic Pancreatitis (CP) and pancreatic ductal adenocarcinoma (PDAC). The generated proximograms were used as inputs to 2 distinct graph deep-learning models. The improved classification results over simpler spatial-data-based input graphs point to the increased discriminatory power obtained by integrating structural information from single-cell ligand-receptor signaling data and the spatial architecture of cells in each disease class, which can help point to markers of high diagnostic significance.

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Publication Details

Journal
Computers in Biology and Medicine
Published
2024-09-09
DOI
https://doi.org/10.1016/j.compbiomed.2024.109082
Citations
5
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
1.17

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article

Proximogram—A multi-omics network-based framework to capture tissue heterogeneity integrating single-cell omics and spatial profiling

Ahmed M. Elhossiny, Sunjong Ji, Santhoshi Krishnan, Arvind Rao et al.
5 citations
Computers in Biology and Medicine
Single-cell and spatial transcriptomics
1.17
article

Proximogram—A multi-omics network-based framework to capture tissue heterogeneity integrating single-cell omics and spatial profiling

Ahmed M. Elhossiny, Sunjong Ji, Santhoshi Krishnan, Arvind Rao, Timothy L. Frankel, Achyutha Rao
article en
5 citations

Abstract

The increasing availability of patient-derived multimodal biological data for various diseases has opened up avenues for finding the optimal methods for jointly leveraging the information extracted in a customizable and scalable manner. Here, we propose the Proximogram, a graph-based representation that provides a joint construct for embedding independently obtained omics and spatial data. To evaluate the representation, we generated proximograms from 2 distinct biological sources, namely, multiplexed immunofluorescence images and single-cell RNA-seq data obtained from patients across two pancreatic diseases that include normal and chronic Pancreatitis (CP) and pancreatic ductal adenocarcinoma (PDAC). The generated proximograms were used as inputs to 2 distinct graph deep-learning models. The improved classification results over simpler spatial-data-based input graphs point to the increased discriminatory power obtained by integrating structural information from single-cell ligand-receptor signaling data and the spatial architecture of cells in each disease class, which can help point to markers of high diagnostic significance.

Computers in Biology and MedicineVol. 182
University of Michigan (US), Michigan Medicine (US), Ann Arbor Center for Independent Living (US)
American Cancer Society, University of Michigan, National Institutes of Health, National Cancer Institute, National Institute of Biomedical Imaging and Bioengineering
Openalex Percentile: Top 22%
Single-cell and spatial transcriptomics
1.17
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